(Q35196369)

7 August 2017

title

Chromosomal origin of small ring marker chromosomes in man: characterization by molecular genetics (English)

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7 August 2017

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Callen DF

1

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7 August 2017

Eyre HJ

2

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7 August 2017

Ringenbergs ML

3

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7 August 2017

Freemantle CJ

4

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7 August 2017

Woodroffe P

5

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7 August 2017

Haan EA

6

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7 August 2017

publication date

1 April 1991

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American Journal of Human Genetics

7 August 2017

language of work or name

English

0 references

published in

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7 August 2017

volume

48

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7 August 2017

issue

4

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7 August 2017

page(s)

769-782

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Human chromosome-specific repetitive DNA sequences: novel markers for genetic analysis

7 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682952

Characterization of human centromeric regions of specific chromosomes by means of alphoid DNA sequences

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682952

Determining the origin of human X isochromosomes by use of DNA sequence polymorphisms and detection of an apparent i(Xq) with Xp sequences

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682952

Homologous subfamilies of human alphoid repetitive DNA on different nucleolus organizing chromosomes

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682952

A novel centromeric repetitive DNA from human chromosome 22.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682952

Isolation and characterization of alphoid DNA sequences specific for the pericentric regions of chromosomes 4, 5, 9, and 19.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682952

The isochromosome 18p syndrome: confirmation of cytogenetic diagnosis in nine cases by in situ hybridization

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682952

Small marker chromosomes in man: origin from pericentric heterochromatin of chromosomes 1, 9, and 16

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682952

Human satellite III DNA: genomic location and sequence homogeneity of the TaqI-deficient polymorphic sequences

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682952

DNA probe localization at 18p113 band by in situ hybridization and identification of a small supernumerary chromosome

26 September 2018

1 reference

12 December 2020

Two subsets of human alphoid repetitive DNA show distinct preferential localization in the pericentric regions of chromosomes 13, 18, and 21

1 reference

12 December 2020

Genomic Organization of Human Centromeric Alpha Satellite DNA: Characterization of a Chromosome 17 Alpha Satellite Sequence

1 reference

12 December 2020

Chromosome-specific alpha satellite DNA: isolation and mapping of a polymorphic alphoid repeat from human chromosome 10

1 reference

12 December 2020

Identifiers

PMC publication ID

1682952

1 reference

7 August 2017

1 reference